RecallRadar

FDA Drug recall D-1531-2022

TRI-MIX 30/2/40 Injectable, 10 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936

On 2022-09-21 the FDA classified a Class II recall of TRI-MIX 30/2/40 Injectable, 10 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936 by Carolina Infusion, citing lack of Assurance of Sterility.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1531-2022
ClassificationClass II
Statuscompleted
Initiated2022-08-26
Published2022-09-21
Last updated2026-09-13 11:52 UTC
CompanyCarolina Infusion
DistributionUS

Product

TRI-MIX 30/2/40 Injectable, 10 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.

Reason

Lack of Assurance of Sterility

Identifiers

code_infoLots: 07152022@4, BUD: 09/13/2022; 08152022@15, BUD: 10/14/2022

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: completed.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1531-2022%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.